A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5544649



Internal ID318776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:36637121..36637288hg38UCSC Ensembl
chr14:37106326..37106493hg19UCSC Ensembl
Cytoband14q13.3
Allele length
AssemblyAllele length
hg38166
hg19166
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17696901
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5544649
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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